Article
[Molecular genetics of hemophilia A].
Medicina - 1 Jan 1996
De Brasi C D, Slavutsky I R, Larripa I B
Abstract excerpt
Hemophilia A (HemA), an X linked genetic disease, is the most common coagulation disorder with an incidence of about 1-2 in 10,000 males and is caused by mutations in the factor VIII (FVIII) coagulation gene. Firstly, some clinical aspects of the HemA are presented: the current methods to assess...
Topics
- Chromosome Inversion
- Factor VIII
- Female
- Genetic Therapy
- Hemophilia A
- Humans
- Male
- Mutation